Tag | Content |
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EnhancerAtlas ID | HS184-25259 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:159865250-159866740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr5:159865545-159865564 | ATGCCACTAGAGGGCACCT | + | 6.26 | CTCF | MA0139.1 | chr5:159866308-159866327 | TGCCCACCAGGGGGCGGCA | + | 7.83 | NFYA | MA0060.3 | chr5:159865947-159865958 | TCTGATTGGTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_32669 | chr5:159865596-159867249 | GM12878 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I160438 | chr5 | 159865208 | 159866890 |
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Enhancer Sequence | ACAGCTCCCA CTAGCAAGAG GTTTGCTGTC AAGGGTGAGA TTTCTGGATT TGTAGTTAGC 60 ACCTTTGGGT TCAGTTCCCA GTTCCACCCT TGACCAGCTG ATCTGACTTT CAGCATGCCA 120 CTTGCCGTTG GCTAAGGCCA GATCCTGAAG GCATCTTCGA TGGTCCACAG AGCAGACAGT 180 AAATTCCCAC TTGCATCTTT GAAGCATCAC TGCCTCCTGC CTCAGTTTAA CAATTGGTTT 240 TGTCCTTCCC TTTGAAAATG AACTGCACTA CCTTTCCTCC CAAGCTAATG TAACCATGCC 300 ACTAGAGGGC ACCTCCTGCC TTCTCAGTCA GTCGCAGCTT CCTCTAATTT GGAAATGATC 360 TTTCAGCTGA GATGGGTGGT ACGTTGGGGT TCGATGTCTT TAGGATTCCT CAGCTTGATG 420 GATGTGGTAA GTTTTGTCCG AAAATCCTGA TTGTTTTTTG CTTTTTCCTT TTTTCTTGTT 480 TTTTTCTTTT ACATCAGACC TCTTTTAATA AAACTGGGGT GGAGAGGTTG GTGGAAGGGA 540 GGGCGCTGTT ACCACCGCCA CCTGACATTG ATAAGTACTT ACTGGCTGCC AGATCAGTGC 600 TAAGTGCCTC ACACGCATCG TCCTTTGGAC TCTCAGAGAA ACGCCATGGG GTGTGGGTAT 660 GCGTGAGCAT TCATTATTGA TGGTTGGAAA CTTGGGCTCT GATTGGTTAA GTAACTTTTG 720 CAACATCCAG CTAGAAGGCA CACTTGGTAC CACGAAGCGG TCTCCATAGA AGCTGGCCTC 780 ACCTGGCTGT TAAGTCAAGC AGGGAGCGGC GGGTCTTGCT GCTCTAGGAC AGTAGTTCTC 840 AGCCTTATCA GACATAAAAG CCCCTTTCTG TATGAAACAT TTCGTAACAC CTCCTGTACT 900 ACCCTGAAGT GATATCCACA GGCAGTGTGT GCCTATGCTT ACATGTCCGC TTACATACAA 960 TGCAAAGGAA ACCTTCTCCT TTTAGGAAAG TATGTCTTAC AAGTATTAGG CTTGTCTATC 1020 TACACCAGAG GACAAAGGTG CCGGGCTAAT TTCGAAACTG CCCACCAGGG GGCGGCATAC 1080 CACATTCCCT GCTGCGATCA GCTCGCACAG ACAGTCCCCC TCCGTGGTGG CTTTGGCTGT 1140 TTCCCCTTCA ACTGGAATTG CCCCGTTAGA CTCTTCCTGA GGTCCCCGGA GTGGCACAGG 1200 GGGTTGTGGT GGAGAGTGAA GCGAAGAAGT CACAGAGCGT GGAGCTGACC CTCATGTTAG 1260 TGTGATAGAT TTCTAGTCAC GTGTACCCAC CATGAGTACA GTCAGATGCT TTAAAATTTT 1320 AGTTTCCTTA CTGAGTGATT TGCTTACAAA GTGATTAGGA AGTAATATGT TTATTTTCAT 1380 TGATACTGCT TTAAAAATTT TTTTATATTA TAGTCAGTGA GCAGTATTCG TTTAATATTT 1440 TTCTTTAAAT CAATTCAATT TTTCTTTAAC ATGAATACAT ATATTTAAAC 1490
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